Quantitative Biophysical Metrics for Rapid Evaluation of Ovarian Cancer Metastatic Potential
dc.contributor.author | Mukherjee, Apratim | en |
dc.contributor.author | Zhang, Haonan | en |
dc.contributor.author | Ladner, Katherine | en |
dc.contributor.author | Brown, Megan | en |
dc.contributor.author | Urbanski, Jacob | en |
dc.contributor.author | Grieco, Joseph P. | en |
dc.contributor.author | Kapania, Rakesh K. | en |
dc.contributor.author | Lou, Emil | en |
dc.contributor.author | Behkam, Bahareh | en |
dc.contributor.author | Schmelz, Eva M. | en |
dc.contributor.author | Nain, Amrinder S. | en |
dc.date.accessioned | 2023-01-25T18:00:25Z | en |
dc.date.available | 2023-01-25T18:00:25Z | en |
dc.date.issued | 2022-05-15 | en |
dc.date.updated | 2023-01-25T17:06:35Z | en |
dc.description.abstract | Ovarian cancer is routinely diagnosed long after the disease has metastasized through the fibrous sub-mesothelium. Despite extensive research in the field linking ovarian cancer progression to increasingly poor prognosis, there are currently no validated cellular markers or hallmarks of ovarian cancer that can predict metastatic potential. To discern disease progression across a syngeneic mouse ovarian cancer progression model, here, we fabricated extracellular-matrix mimicking suspended fiber networks: crosshatches of mismatch diameters for studying protrusion dynamics, aligned same diameter networks of varying inter-fiber spacing for studying migration, and aligned nanonets for measuring cell forces. We found that migration correlated with disease, while force-disease biphasic relationship exhibited f-actin stress-fiber network dependence. However, unique to suspended fibers, <i>coiling</i> occurring at tips of protrusions and not the length or breadth of protrusions displayed strongest correlation with metastatic potential. To confirm that our findings were more broadly applicable beyond the mouse model, we repeated our studies in human ovarian cancer cell lines and found that the biophysical trends were consistent with our mouse model results. Altogether, we report complementary high throughput and high content biophysical metrics capable of identifying ovarian cancer metastatic potential on time scale of hours. | en |
dc.description.version | Published version | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.doi | https://doi.org/10.1091/mbc.e21-08-0419 | en |
dc.identifier.eissn | 1939-4586 | en |
dc.identifier.issn | 1059-1524 | en |
dc.identifier.issue | 6 | en |
dc.identifier.orcid | Kapania, Rakesh [0000-0001-7294-4703] | en |
dc.identifier.orcid | Behkam, Bahareh [0000-0002-2174-2914] | en |
dc.identifier.orcid | Nain, Amrinder [0000-0002-9757-2341] | en |
dc.identifier.orcid | Schmelz, Eva [0000-0002-3374-5266] | en |
dc.identifier.pmid | 34985924 | en |
dc.identifier.uri | http://hdl.handle.net/10919/113424 | en |
dc.identifier.volume | 33 | en |
dc.language.iso | en | en |
dc.publisher | American Society for Cell Biology | en |
dc.relation.uri | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000800657800011&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=930d57c9ac61a043676db62af60056c1 | en |
dc.rights | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International | en |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | en |
dc.subject | Science & Technology | en |
dc.subject | NANONET FORCE MICROSCOPY | en |
dc.subject | HUMAN MESOTHELIAL CELLS | en |
dc.subject | EXTRACELLULAR-MATRIX | en |
dc.subject | TUMOR-METASTASIS | en |
dc.subject | FOCAL ADHESIONS | en |
dc.subject | MYOSIN-II | en |
dc.subject | IN-VITRO | en |
dc.subject | MIGRATION | en |
dc.subject | PROGRESSION | en |
dc.subject | SINGLE | en |
dc.subject | Rare Diseases | en |
dc.subject | Ovarian Cancer | en |
dc.subject | Cancer | en |
dc.subject.mesh | Cell Line, Tumor | en |
dc.subject.mesh | Extracellular Matrix | en |
dc.subject.mesh | Animals | en |
dc.subject.mesh | Humans | en |
dc.subject.mesh | Mice | en |
dc.subject.mesh | Ovarian Neoplasms | en |
dc.subject.mesh | Actins | en |
dc.subject.mesh | Cell Movement | en |
dc.subject.mesh | Benchmarking | en |
dc.subject.mesh | Female | en |
dc.title | Quantitative Biophysical Metrics for Rapid Evaluation of Ovarian Cancer Metastatic Potential | en |
dc.title.serial | Molecular Biology of the Cell | en |
dc.type | Article - Refereed | en |
dc.type.dcmitype | Text | en |
dc.type.other | Article | en |
dcterms.dateAccepted | 2021-11-29 | en |
pubs.organisational-group | /Virginia Tech | en |
pubs.organisational-group | /Virginia Tech/Agriculture & Life Sciences | en |
pubs.organisational-group | /Virginia Tech/Agriculture & Life Sciences/Human Nutrition, Foods, & Exercise | en |
pubs.organisational-group | /Virginia Tech/Engineering | en |
pubs.organisational-group | /Virginia Tech/Engineering/Aerospace and Ocean Engineering | en |
pubs.organisational-group | /Virginia Tech/Engineering/Mechanical Engineering | en |
pubs.organisational-group | /Virginia Tech/Faculty of Health Sciences | en |
pubs.organisational-group | /Virginia Tech/All T&R Faculty | en |
pubs.organisational-group | /Virginia Tech/Engineering/COE T&R Faculty | en |
pubs.organisational-group | /Virginia Tech/Agriculture & Life Sciences/CALS T&R Faculty | en |
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